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Study on the Association between Silent aspiration and Chronic Obstructive Pulmonary Disease (COPD) exacerbation

Study on the Association between Silent aspiration and Chronic Obstructive Pulmonary Disease (COPD) exacerbation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-CCH-12002918
Enrollment
Unknown
Registered
2012-12-18
Start date
2012-06-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease (COPD) exacerbation

Interventions

Sponsors

The First Affiliated Hospital of Guangzhou Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 90 Years

Inclusion criteria

Inclusion criteria: Patients with AECOPD and age-matched COPD-free controls, who were hospitalized in the First Affiliated Hospital of Guangzhou Medical College from June 2012 to December 2012, were recruited in this study. Written informed consent forms were obtained from all participants. The inclusion criteria were as follows: 1. >=50 years of age; 2. a smoking history of >=30 packs of cigarettes per year; 3. a medical history and results of physical examination, chest radiography, and pulmonary function test (PFT) consistent with the diagnosis of COPD (In particular, the result of PFT should include an FEV1/FVC ratio <=70%); 4. a COPD exacerbation event defined as an acute event characterized by significant worsening of the respiratory symptoms that led to a change in medication.

Exclusion criteria

Exclusion criteria: 1. patients with respiratory complications other than COPD; 2. patients with previous experience of tracheostomy, patients with head and neck cancer or with previous experience of head and neck surgery, and patients with CNS muscle pathology; 3. patients who underwent endotracheal incubation within 3 months; 4. patients with esophageal diseases, including cancer and stricture.

Design outcomes

Secondary

MeasureTime frame
BMI data, MRC scores, arterial blood gases and blood cell counts, chest radiography;

Primary

MeasureTime frame
Frequency of exacerbation events with 1 year (times);

Countries

China

Contacts

Public ContactZeguang Zheng
zheng8620@yahoo.com.cn+86 13719168238

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026